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Synthesis of 1,4-diketones by the coupling reaction of trimethylsilyl enol ethers with lead tetraacetate

โœ Scribed by Robert M. Moriarty; Raju Penmasta; Indra Prakash


Publisher
Elsevier Science
Year
1987
Tongue
French
Weight
183 KB
Volume
28
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


Synthesis of 1,4-diketones in good yields was achieved by the coupling reaction of the trinethylsilyl enol ethers of acetophenone, thiophene or furan with lead tetraacetate in dry dichloromethane and tetrahydrofuran at -78"C.


๐Ÿ“œ SIMILAR VOLUMES


Facile synthesis of silyl enol ethers by
โœ Yoshio Ishino; Yoshio Kita; Hirofumi Maekawa; Toshinobu Ohno; Yasuhiro Yamasaki; ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 225 KB

Treatment of aliphatic carbonyl compounds with trimethyisilyl chloride with Mg turning for Grignard reaction without any pre-treatmem in N,N-dimethylformamide at room temperature brought about highly facile, effective and stereoselective coupling to give the corresponding silyl enol ethers in good y